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Article

A method for the analysis of 32 X chromosome insertion deletion polymorphisms in a single PCR.

International journal of legal medicine - 1 Jan 2012

Pereira Rui, Pereira Vânia, Gomes Iva, Tomas Carmen, Morling Niels, Amorim António, Prata Maria João, Carracedo Angel, Gusmão Leonor

Abstract excerpt

Studies of human genetic variation predominantly use short tandem repeats (STRs) and single nucleotide polymorphisms (SNPs) but Insertion deletion polymorphisms (Indels) are being increasingly explored. They combine desirable characteristics of other genetic markers, especially the possibility of being analysed using short amplicon strategies, which increases the ease of analysis, contributing to justify their...

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PMID: 21717151
DOI: 10.1007/s00414-011-0593-2

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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